Title
Quality of life improvement in resource-limited settings after one year of second-line antiretroviral therapy use among adult men and women
Date Issued
13 March 2018
Access level
metadata only access
Resource Type
journal article
Author(s)
Torres T.S.
Harrison L.J.
Cardoso S.W.
Zheng L.
Ngongondo M.
Some F.
Lalloo U.G.
Mwelase T.
Collier A.C.
Hughes M.D.
Publisher(s)
Lippincott Williams and Wilkins
Abstract
Objective: We evaluated improvement of quality of life (QoL) after 1 year of second-line antiretroviral therapy (ART) use in resource-limited settings (RLS) among adult men and women, comparing two randomized treatment arms. Design: The AIDS Clinical Trial Group A5273 was a randomized clinical trial of second-line ART comparing lopinavir/ritonavir (LPV/r) + raltegravir with LPV/r + nucleos(t)ide reverse transcriptase inhibitors (NRTIs) in participants failing a non-NRTI-containing regimen at 15 sites in nine RLS. Participants completed the AIDS Clinical Trial Group short-form-21 which has eight QoL domains with a standard score ranging from 0 (worst) to 100 (best). Methods: Differences in QoL by randomized arm, as well as by demographic and clinical variables, were evaluated by regression models for baseline and week 48 QoL scores fitted using the generalized estimating equations method. Results: A total of 512 individuals (49% men, median age 39 years) were included. A total of 512 and 492 participants had QoL assessments at baseline and week 48, respectively. QoL improved significantly from baseline to week 48 (P < 0.001 for all domains). There was no significant difference between treatment arms for any domain. Individuals with higher viral load and lower CD4 + cell count at baseline had lower mean QoL at baseline but larger improvements such that mean QoL was similar at week 48. Conclusion: Improvements in QoL were similar after starting second-line ART of LPV/r combined with either raltegravir or NRTIs in RLS. QoL scores at baseline were lower among participants with worse disease status prior to starting second-line, but after 1 year similar QoL scores were achieved.
Start page
583
End page
593
Volume
32
Issue
5
Language
English
OCDE Knowledge area
Virología Enfermedades infecciosas
Scopus EID
2-s2.0-85044191830
PubMed ID
Source
AIDS
ISSN of the container
02699370
Sponsor(s)
S. Poongulali, Chennai Antiviral Research and Treatment Clinical Research Center (CRS), Chennai, India; Metch Matoga, Malawi CRS, Lilongwe, Malawi; Anthony Chisada, Parirenyatwa CRS, Harare, Zimbabwe; Fatma Faraj Some, Moi University CRS, Eldoret, Kenya; U.G.L., Durban International CRS, Durban, South Africa; Mohammed Siddique Rassool, University of Witwatersrand Helen Joseph CRS, Johannesburg, South Africa; Dileep Babasaheb Kadam, Byramjee Jeejeebhoy Government Medical College CRS, Pune, India; Lerato Mohapi, Soweto ACTG CRS, Soweto, South Africa; Venance Maro, Kilimanjaro Christian Medical Center CRS, Moshi, Tanzania; Mulinda Nyirenda, Blantyre CRS and Johns Hopkins Research Project Blantyre, Malawi; Raman Raghunathrao Gangakhedkar, Pune CRS, Pune, India; S.W.C., Instituto Nacional de Infectologia Evandro Chagas (INI-Fiocruz), Rio de Janeiro, Brazil; Khuanchai Supparatpinyo, Chiang Mai University, Chiang Mai, Thailand; Mey Leon, Barranco CRS, Lima, Peru; John MacRae, San Miguel CRS, Lima, Peru. ACTG A5273 study was supported National Institute of Allergy and Infectious Diseases (award number U01AI068636), National Institute of Mental Health (NIMH) and the National Institute of Dental and Craniofacial Research (NIDCR). The study was also funded via the following grants: AI069432, AI069438, AI069481, AI27757, 2UM1AI069423 (including a subcontract to the Pittsburgh Virology Specialty Laboratory), UM1 AI069471 and UM1 AI068634 (ACTG Statistical and Data Management Center) and the Investigator-Initiated Studies Program of Merck Sharp & Dohme. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Allergy and Infectious Diseases, the National Institutes of Health or Merck Sharp & Dohme. Abbott Laboratories, Gilead Sciences, ViiVHealthcare/GSK and Merck Sharp & Dohme provided the study drugs.
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